Improving person – centered healthcare pathway organization for people with Parkinson’s disease, using Article 51.
Objective: To optimize efficacy and efficiency of the healthcare pathway (HCPW) for people with Parkinson’s disease (PwPD), using the political framework Article 51. Background: Parkinson’s…Catatonia, Parkinsonism and Dystonia in a patient with Osmotic Demyelination Syndrome
Objective: We present a case of Osmotic Demyelination Syndrome (ODS) in a patient who underwent liver transplant and subsequently developed multiple movement disorders. Background: ODS…Incidence of Hip Fracture in People with Parkinson’s Disease at the Tertiary Care Hospital
Objective: This study aims to highlight the incidence of hip fracture in people with Parkinson’s disease. Background: Fall related injuries represent the most frequent reason…Customizing Rehabilitation based on oromotor function assessed with dynamic MRI in early Parkinson’s disease
Objective: Observing subtle oromotor signs (if any) and planning rehabilitation in early stage PD. Background: Dysphagia is a common oromotor symptom in PD but is…Bilateral vocal cord paralysis associated with idiopathic Parkinson’s disease
Objective: We present two cases of bilateral vocal cord paralysis (BVCP) associated with idiopathic Parkinson’s disease (iPD). Background: BVCP is a rare complication associated with…The effect of Deep Brain Stimulation in patients with Parkinson’s Disease on the Brain Cognitive Functions
Objective: To evaluate the effect of Deep Brain Stimulation (DBS) on cognitive functions and affective symptoms in patients with Parkinson's Disease (PD). Background: DBS helps…Gender differenes in cognitive functioning in de novo Parkinson’s disease patients
Objective: To clarify the differences in cognitive functioning across different cognitive domains, between male and female de novo PD patients. Background: Parkinson’s disease (PD) is…Optic atrophy and parkinsonism in a family associated with OPA1 mutation
Objective: To report a Taiwanese family with a heterozygous missense mutation of OPA1 gene (NM_130836, p.Ser582Arg) presenting with optic atrophy and parkinsonism and establish an…Whole exome trio analysis in isolated population of southeast Moravia (Czech Republic) with familial parkinsonism suggests its heterogeneous genetic background
Objective: The aim of the study was to identify shared genetic variants potentially associated with familial neurodegenerative parkinsonism using whole-exome analysis. Background: Increased prevalence of…ADAM10 polymorphisms are not associated with susceptibility to Parkinson’s disease and Parkinson’s disease with cognitive impairment in a Chinese cohort
Objective: This study is to explore the relationship between the rs442495 and rs593742 loci of ADAM10 gene and Parkinson's disease( PD) or PD cognitive impairment.…
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